Peter Phillips serves as the Chief Operating Officer at BlueDop Medical, where he leverages over 30 years of leadership in the medical device and healthcare industries. Before stepping into his current role, Peter contributed as a Non-Executive Director on BlueDop’s Board, bringing strategic oversight and valuable governance. He continues to expand his influence in the industry as a Non-Executive Director at EXSTENT, underlining his expertise in guiding medical device companies to success.

Peter’s distinguished career includes key leadership positions such as CEO of OxVent and Managing Director at Lombard Medical, where he spearheaded the European launch of pioneering medical products and played a critical role in fundraising and IPOs. His tenure as Chief Technology Officer at Lombard Medical Ltd involved overseeing clinical studies, regulatory compliance, and intellectual property management, showcasing his proficiency in operational strategy and FDA compliance. With a robust background in corporate strategy, commercialization, and board-level leadership, Peter is dedicated to driving operational excellence and strategic growth at BlueDop Medical.

Ross Robinson brings over 20 years of clinical experience in podiatry, having worked across various leadership roles within the NHS and the private sector. His expertise includes managing high-risk diabetic patients, creating innovative clinical programs, and reducing patient waiting times. In addition, Ross has over 6 years of experience in the medical industry, where he has taken on roles such as EMEA Business Manager and Vice President of Medical Affairs. His industry experiences spans managing scientific communications, regulatory compliance, and medical content related to medical devices, as well as forging key relationships with healthcare professionals and industry leaders globally.

Jo Cronin-Wojdat is the Head of Quality & Regulatory at BlueDop Medical, bringing over 20 years of experience in many aspects of Quality Management, Regulatory Affairs, and Operational oversight within Medical Devices, Life Sciences and Pharmaceuticals. She has developed and implemented Quality Management Systems (QMS) and regulatory frameworks for numerous organizations, including large global corporations such as Thermo Fisher Scientific, Imperial Brands and ConvaTec. Jo specializes in ensuring compliance with international standards including ISO standards and FDA requirements whilst maintaining an overview of new emerging requirements.  She has successfully implemented many operational excellence improvements, with demonstrable time and cost savings.  Jo has extensive experience of Customer and regulatory audits and inspections, including FDA, UK, and global agencies.